Kalantari Nasim, Abroun Saeid, Soleimani Masoud, Kaviani Saeid, Azad Mehdi, Eskandari Fatemeh, Habibi Hossein
Department of Hematology and Blood Banking, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Department of Medical Laboratory Sciences, Faculty of Allied Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
Cell J. 2016 Fall;18(3):322-31. doi: 10.22074/cellj.2016.4559. Epub 2016 Aug 24.
Receptor activator of nuclear factor-kappa B ligand (RANKL) appears to be an osteoclast-activating factor, bearing an important role in the pathogenesis of multiple myeloma. Some studies demonstrated that U-266 myeloma cell line and primary myeloma cells expressed RANK and RANKL. It had been reported that the expression of myeloid and monocytoid markers was increased by co-culturing myeloma cells with hematopoietic stem cells (HSCs). This study also attempted to show the molecular mechanism of RANK and RANKL on differentiation capability of human cord blood HSC to osteoclast, as well as expression of calcitonin receptor (CTR) on cord blood HSC surface.
In this experimental study, CD133(+) hematopoietic stem cells were isolated from umbilical cord blood and cultured in the presence of macrophage colony-stimulating factor (M-CSF) and RANKL. Osteoclast differentiation was characterized by using tartrate-resistant acid phosphatase (TRAP) staining, giemsa staining, immunophenotyping, and reverse transcription-polymerase chain reaction (RT-PCR) assay for specific genes.
Hematopoietic stem cells expressed RANK before and after differentiation into osteoclast. Compared to control group, flow cytometric results showed an increased expression of RANK after differentiation. Expression of CTR mRNA showed TRAP reaction was positive in some differentiated cells, including osteoclast cells.
Presence of RANKL and M-CSF in bone marrow could induce HSCs differentiation into osteoclast.
核因子κB受体活化因子配体(RANKL)似乎是一种破骨细胞活化因子,在多发性骨髓瘤的发病机制中起重要作用。一些研究表明,U-266骨髓瘤细胞系和原发性骨髓瘤细胞表达RANK和RANKL。据报道,将骨髓瘤细胞与造血干细胞(HSCs)共培养可增加髓系和单核细胞标志物的表达。本研究还试图揭示RANK和RANKL对人脐血造血干细胞向破骨细胞分化能力的分子机制,以及脐血造血干细胞表面降钙素受体(CTR)的表达情况。
在本实验研究中,从脐血中分离出CD133(+)造血干细胞,并在巨噬细胞集落刺激因子(M-CSF)和RANKL存在的情况下进行培养。通过抗酒石酸酸性磷酸酶(TRAP)染色、吉姆萨染色、免疫表型分析以及针对特定基因的逆转录-聚合酶链反应(RT-PCR)检测来表征破骨细胞分化情况。
造血干细胞在分化为破骨细胞之前和之后均表达RANK。与对照组相比,流式细胞术结果显示分化后RANK表达增加。CTR mRNA的表达表明TRAP反应在一些分化细胞(包括破骨细胞)中呈阳性。
骨髓中RANKL和M-CSF的存在可诱导造血干细胞分化为破骨细胞。